Our Experienced Staff and Network Respond to a Variety of Needs
Our experienced staff respond to various needs for pharmaceutical development. Utilizing our network, we also support licensing plans from overseas and clinical development in Europe, the USA and Asia.

【Consultation 】
- ・Planning of Development Strategy, Clinical Trial Plans, and Various Reviews
- ・Consultation for Licensing in from Overseas and for Clinical Trials in Foreign Countries
- ・Regulatory Consultation
- ・Other General Consultation for Development of Drugs and Medical Devices
【Activity Support】
- ・Support for Organization and Operation of Standard Operating Procedures (SOPs)
- ・Support for Consultation with the Regulatory Authority (Pharmaceuticals and Medical Devices Agency)
- ・Support for Protocol Development and Development of Informed Consent
- ・Representative Service in Regulation and Support for Regulatory Applications
【Others】
- ・Support for Studies in Humans on Health Food and Health Supplements
- ・Support for Investigator-Initiated Clinical Trials, Large-Scale Epidemiological Studies, etc.
- ・Support for Bioequivalence Studies on Generic Drugs and Applications
- We are able to provide consulting services specialized in various therapeutic areas such as carcinoma diseases, cardiovascular diseases and central nerve system diseases.
- We are flexible to your needs, from representative service in regulation to phamaceutical and medical device consultation.
[ Contact ] Sales Department TEL +81-3-5804-7577 / FAX +81-3-5684-7872
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